Process for the production of atorvastatin calcium

ABSTRACT

In one aspect, the invention provides a process for the production of 5-(4-Fluoro-phenyl)-2-isopropyl-4-phenyl-1-(3,5,7-trihydroxy-heptyl)-1H-pyrrole-3-carboxylic acid phenylamide hemicalcium salt, stereoisomers thereof or polymorphs thereof from a (6-{2-[2-(4-Fluoro-phenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoyl-pyrrolidin-1-yl]-ethyl}-2-phenyl-[1,3,2]dioxaborinan-4-yl)-acetic acid tert-butyl ester.

PRIORITY CLAIM

The present application claims the benefit under 35 U.S.C. § 371 of International Application No.: PCT/IN03/00328, filed Oct. 7, 2003, the entire contents of this application is hereby incorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to a novel process for the production of atorvastatin calcium. Particularly, the present invention relates to a novel process for the production of amorphous atorvastatin calcium from (6-{2-[2-(4-Fluoro-phenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoyl-pyrrolidin-1-yl]-ethyl}-2-phenyl-[1,3,2]dioxaborinan-4-yl)-acetic acid tert-butyl ester.

BACKGROUND OF THE INVENTION

Atorvastatin calcium is known by synonyms like [R-(R*,R*)]-2-(4-fluorophenyl)-σσ, 6-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino) carbonyl-1H-pyrrole-1-heptanoic acid hemicalcium salt; (δR,δR)-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid hemicalcium salt; [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid hemicalcium salt or (βR,δR)-2-(p-Fluorophenyl)-β,δ-dihydroxy-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)pyrrole-1-heptanoic acid hemicalcium salt.

The hemicalcium salt of [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid, a synthetic HMG-CoA reductase inhibitor, is used for the treatment of hyperlipidemia and hypercholesterolemia, both of which are risk factors for arteriosclerosis and coronary heart disease. Open dihydroxy carboxylic acid, lactone and various salt forms of [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid have been synthesized.

U.S. Pat. No. 5,273,995, teaches that [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid has surprising inhibition of the biosynthesis of cholesterol. The calcium salt of [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid (2:1) (Formula I)

is more suited to formulations and has been recommended as a drug.

U.S. Pat. Nos. 5,003,080; 5,097,045; 5,103,024; 5,124,482; 5,149,837; 5,155,251; 5,216,174; 5,245,047; 5,248,793; 5,273,995; 5,280,126; 5,298,627; 5,342,952; 5,385,929; 5,397,792; European Patent 409,281; and WO 89/07598 describe various processes and key intermediates for preparing atorvastatin.

WO 97/03958 and WO 97/03959 disclose novel crystalline forms of atorvastatin calcium designated as Form I, Form II, Form III and Form IV and methods for their preparation, providing more favorable filtration and drying characteristics.

WO 97/03960 and U.S. Pat. No. 6,087,511 describe procedures for converting the crystalline form of atorvastatin calcium to an amorphous form. The processes disclosed therein involve dissolving Form I atorvastatin calcium in a non-hydroxylic solvent like tetrahydrofuran or a mixture of tetrahydrofuran and toluene.

WO 00/71116 describes a procedure for converting the crystalline Form-I by dissolving it in a non-hydroxylic solvent like tetrahydrofuran and precipitating amorphous atorvastatin calcium by the addition of nonpolar hydrocarbon solvents like, n-hexane, cyclohexane or n-heptane, for example.

It is therefore one object of the present invention to provide a novel process for the preparation of atorvastatin calcium, unique with respect to its simplicity, cost effectiveness and scalability.

SUMMARY OF THE INVENTION

The present invention relates to a novel process for the preparation of atorvastatin calcium.

In one aspect, the process of the present invention comprises converting a compound of Formula II to atorvastatin calcium (Formula I).

In certain exemplary embodiments, the process comprises treating a compound of Formula II with calcium oxide.

The process of the present invention is novel, simple, inexpensive and industrially scalable.

Advantages of the present invention include: de-protection of a boronate ester, cleavage of a tert-butyl ester and formation of a calcium salt are achieved in one step, employing a single reagent; a simple procedure involving inexpensive CaO is used; and calcium salt is obtained directly without the need for making sodium salt or any other intermediates, thereby reducing the necessary number of steps.

DETAILED DESCRIPTION OF CERTAIN PREFERRED EMBODIMENTS OF THE INVENTION

In certain embodiments, the novel process of the present invention relates to the preparation of [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid hemicalcium salt.

In one aspect, the process is a simple, one-step, economic and industrially scalable process comprising converting (6-{2-[2-(4-Fluoro-phenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoyl-pyrrolidin-1-yl]-ethyl}-2-phenyl-[1,3,2]dioxaborinan-4-yl)-acetic acid tert-butyl ester to [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid hemicalcium, its stereoisomers or polymorphic forms.

In one embodiment, the process comprises treating (6-{2-[2-(4-Fluoro-phenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoyl-pyrrolidin-1-yl]-ethyl}-2-phenyl-[1,3,2]dioxaborinan-4-yl)-acetic acid tert-butyl ester with calcium oxide in a suitable solvent.

In another embodiment, a suitable solvent is selected from water, water miscible or water immiscible solvent.

In certain embodiments, the solvent system used may be a single solvent or a mixture of two or more solvents.

In certain other embodiments, the water miscible solvent may be selected from one or more among methanol, ethanol, isopropanol, acetone, THF or acetonitrile, or a combination thereof.

In another aspect, the reaction of the present invention is carried out at suitable reaction conditions required for satisfactory conversion of the starting material to atorvastatin calcium. In one embodiment, the starting material is Formula II.

In yet another aspect, the reaction may be carried out at a temperature between about 25 to 100° C. In one embodiment of this aspect, the reaction is carried out at a temperature between about 40 to 70° C.

The reaction may be carried out for a time period between about 1 to 24 hours. In one embodiment, the reaction is carried out for a time period between about 5 to 15 hours.

After satisfactory conversion, the product may be isolated with or without further purification.

The present invention will now be illustrated by the following examples, which are not intended to limit the effective scope of the claims. Consequently, any variations of the invention described above are not to be regarded as departure from the spirit and scope of the invention as claimed. The present invention has been described in terms of its specific embodiments and various modifications and equivalents will be apparent to those skilled in the art and are intended to be included within the scope of present invention.

EXAMPLE 1

A mixture of (6-{2-[2-(4-Fluoro-phenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoyl-pyrrolidin-1-yl]-ethyl}-2-phenyl-[1,3,2]dioxaborinan-4-yl)-acetic acid tert-butyl ester (5 g, 0.007 mol), water (200 ml), methanol (200 ml) and calcium oxide (5.0 g, 0.09 mol) was stirred at 50-60° C. for 10 hours. After filtering the reaction mixture, the resulting clear filtrate was concentrated to about 150 ml and washed with methyl tert-butyl ether (50 ml). The aqueous layer was evaporated and the solid obtained was dissolved in THF (50 ml). The solution was filtered and concentrated to yield [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid hemicalcium salt.

EXAMPLE 2

A mixture of (6-{2-[2-(4-Fluoro-phenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoyl-pyrrolidin-1-yl]-ethyl}-2-phenyl-[1,3,2]dioxaborinan-4-yl)-acetic acid tert-butyl ester (50 g, 0.07 mol), water (2 L), THF (2 L) and calcium oxide (50 g, 0.9 mol) was stirred at 50-60° C. for 8 hours. After filtering the reaction mixture, the resulting clear filtrate was concentrated to about 1.5 L and washed with methyl tert-butyl ether (500 ml). The aqueous layer was evaporated and solid obtained was dissolved in THF (500 ml). The solution was filtered and concentrated to yield atorvastatin calcium.

EXAMPLE 3

A mixture of (6-{2-[2-(4-Fluoro-phenyl)-5-isopropyl-3-phenyl-4-phenylcarbamoyl-pyrrolidin-1-yl]-ethyl}-2-phenyl-[1,3,2]dioxaborinan-4-yl)-acetic acid tert-butyl ester (100 g, 0.14 mol), water (3.0 L), acetonitrile (3.0 L) and calcium oxide (75 g, 1.35 mol) was stirred at 50-60° C. for 12 hours. After filtering the reaction mixture, the resulting clear filtrate was concentrated to about 3.0 L and washed with methyl tert-butyl ether (1.0 L). The aqueous layer was evaporated and the solid obtained was dissolved in acetonitrile (1.0 L). The solution was filtered and concentrated to yield [R-(R*R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, 1H-Pyrrole-1-heptanoic acid hemicalcium salt. 

1. A novel process for the preparation of a compound of Formula I′

the process comprising: treating a compound of Formula II

with a source of calcium ion.
 2. The process of claim 1, wherein the source of calcium ion is a suitable calcium ion.
 3. The process of claim 1, wherein the reaction is carried out in a suitable solvent.
 4. The process of claim 3, wherein the solvent is water, a water miscible solvent or a water immiscible solvent.
 5. The process of claim 3, wherein the solvent is water or a water miscible solvents.
 6. The process of claim 4, wherein the water miscible solvent is a dielectric polar solvent.
 7. The process of claim 6, wherein the dielectric polar solvent is methanol, ethanol, isopropanol, acetone, acetonitrile or THF.
 8. The process of claim 1, wherein the reaction is carried out at a temperature between about 25 to 140° C.
 9. The process of claim 8, wherein the reaction is carried out at a temperature between about 40 to 80° C.
 10. process of claim 1, wherein the reaction is carried out for a time period between about 0 to 24 hour.
 11. The process of claim 1, wherein the reaction is carried out for a time period between about 1 to 10 hour.
 12. The process of claim 1, wherein the compound of Formula I′ is afforded by precipitation or crystallization.
 13. The process of claim 1, wherein the compound of Formula I′ is in amorphous state.
 14. The process of claim 1, wherein the compound of Formula I′ is in crystalline state.
 15. The process of claim 1, wherein the compound of Formula I′ has the structure


16. (canceled)
 17. (canceled)
 18. The process of claim 2, wherein the compound of calcium is CaO or Ca(OH)₂. 